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Clinical Characteristics of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis in Carriers of a Leber Hereditary Optic Neuropathy Variant

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机构： [1]Beijing Tongren Eye Center , Beijing Tongren Hospital, Capital Medical University, Beijing, China [2]Beijing Ophthalmology and Visual Sciences Key Laboratory , Beijing, China [3]Centre for Ophthalmology and Visual Science , The University of Western Australia, Perth, Washington, Australia [4]Ophthalmology, Department of Surgery, University of Melbourne, Melbourne, VIC, Australia [5]and Department of Ophthalmology , Royal Perth Hospital, Perth, Washington, Australia [6]Beijing Tongren Eye center, Beijing Tongren Hospital, Capital Medical University [7]Beijing Ophthalmology and Visual Sciences Key Laboratory, Beijing, China.

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One in a 1,000 population carries one of Leber hereditary optic neuropathy (LHON) mtDNA pathogenic variants1 while one in 40,000–76,000 population has myelin oligodendrocyte glycoprotein antibodyassociated disorder (MOGAD).2 Although simultaneous LHON and MOG-related optic neuritis (MOG-ON) are exceedingly rare3,4, their co-occurrence raises the question of coincidental pathology. We report 3 MOG-ON cases in patients with LHON-associated mitochondrial DNA (mtDNA) pathogenic variants, comparing the clinical features.

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出版当年[2025]版：

大类 | 4 区医学

小类 | 4 区临床神经病学 4 区眼科学

最新[2025]版：

大类 | 4 区医学

小类 | 4 区临床神经病学 4 区眼科学

第一作者：

第一作者机构： [1]Beijing Tongren Eye Center , Beijing Tongren Hospital, Capital Medical University, Beijing, China [2]Beijing Ophthalmology and Visual Sciences Key Laboratory , Beijing, China

通讯作者：

通讯机构： [1]Beijing Tongren Eye Center , Beijing Tongren Hospital, Capital Medical University, Beijing, China [2]Beijing Ophthalmology and Visual Sciences Key Laboratory , Beijing, China

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